Randomized Comparison of 2 Fixation Techniques for Unstable Intertrochanteric Hip Fractures (EMvsIM)
Primary Purpose
Hip Fractures
Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Dynamic Hip Screw (DHS); Trochanteric Fixation Nail (TFN)
Sponsored by
About this trial
This is an interventional treatment trial for Hip Fractures focused on measuring intertrochanteric fractures
Eligibility Criteria
Inclusion Criteria:
- 55 years or older
- Type A2 Intertrochanteric fractures
- Mono trauma
- Medically fit for surgery
- Less than 2 weeks post fracture
Exclusion Criteria:
- Fractures due to malignancy
- Non-ambulatory pre-fracture
- Severe dementia
- Limited life expectancy due to significant medical co-morbidities
- Medical contraindication to surgery
- Inability to comply with rehabilitation of form completion
Sites / Locations
- McGill University Health Centre - Montreal General Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
EM device
IM device
Arm Description
Extramedullary Device (EM)
Intramedullary Device (IM)
Outcomes
Primary Outcome Measures
Timed 2 minute walking distance
TUG (Time up and go) test
Trendelenburg's test: pelvic drop
Fracture classification: Mueller/ AO, displacement, time to union, heterotopic ossification and shortening.
FIM (Functional Independence Measure)
LEM (Lower Extremity Measure)
Secondary Outcome Measures
Secondary Outcome Variable: Transfusions
Pre and Post operative Hgb
Complications/ Re-operation
Length of surgery and hospital stay
Weight bearing status post-op
Full Information
NCT ID
NCT00597779
First Posted
January 9, 2008
Last Updated
August 14, 2014
Sponsor
Rudy Reindl
Collaborators
Orthopaedic Trauma Association
1. Study Identification
Unique Protocol Identification Number
NCT00597779
Brief Title
Randomized Comparison of 2 Fixation Techniques for Unstable Intertrochanteric Hip Fractures
Acronym
EMvsIM
Official Title
Extramedullary vs. Intramedullary Devices in the Treatment of Unstable Intertrochanteric Hip Fractures
Study Type
Interventional
2. Study Status
Record Verification Date
August 2014
Overall Recruitment Status
Completed
Study Start Date
February 2007 (undefined)
Primary Completion Date
November 2012 (Actual)
Study Completion Date
November 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Rudy Reindl
Collaborators
Orthopaedic Trauma Association
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to compare the clinical and radiological outcome of patients that are treated with two different orthopedic implants. The study population will consist of patients that have sustained unstable hip fractures. The two different implants will be randomly assigned.
The null hypothesis states that there should not be any significant differences between the two implants.
Detailed Description
Intertrochanteric hip fractures are common injuries in the elderly population. They often signify generalized physical deterioration. Operative management has become the standard of care to prevent life threatening complications and dates back to the 1940's. The design of implants has evolved significantly since then.
The sliding hip screw replaced static fixation of the femoral head in the 1950's. As a result of this improvement in design, failures have been reduced to 9-16%. The sliding hip screw allows for stable collapse of the femoral neck. This can lead to significant shortening of the proximal femur in comminuted fractures.
Current treatment modalities focus on obtaining a satisfactory union of the fracture, often at the expense of anatomical alignment. Severely comminuted fractures treated with a standard plate-hip-screw device thus commonly result in significant degrees of mal-union and shortening. In the past, implants designed to restore and maintain the anatomy of the hip have resulted in high failure rates with the implant breaking out of the femoral head. In the mid 1980's, recognition of this led to the development of various intramedullary devices for fixation of these fractures. The weight-bearing portion of the implant is therefore shifted medially, resulting in reduced lever forces on the implant and femur. Additionally, the IM device does not rely on fixation to the lateral cortex of the femur with screws. From a biomechanical standpoint, the intramedullary device has distinct advantages, as it is a load- sharing device more closely located to the axis of weight bearing than the plate-hip-screw device.
Advances in intramedullary designs have been promising, but the clinical results variable. The relatively high rate of fracture at the tip, specifically at the level of the locking bolts, has hampered the widespread popularity of intramedullary devices. Additionally, the large diameter of the proximal aspect of the implants required extensive reaming of the greater trochanter and partial detachment of the gluteus medius. This may lead to abductor weakness and a Trendelenburg gait. Some studies have found increased re-operation rates for these early hip-nail devices compared to the plate -hip-screw implant. Other studies have shown decreased blood loss and operative time with the nails. A meta-analysis of the literature favors the sliding hip screw design. Unfortunately, most studies focus on radiological failure rate rather than patient function and relate to the first generation of IM devices.
The newest generation of nails (like the IM studied here) has attempted to correct the shortcomings of earlier designs. The proximal aspect of the nail diameter is minimized. The distal locking screw is located far away from the distal end of the nail and the locking bolt is placed in an oblique fashion. Design alterations to the femoral head fixation portion of the nail by using a helical blade rather than a screw may improve fixation in the femoral head. These new designs seem to compare favorably in recent clinical tests. Early mobilization for patients with the intramedullary device (IM) seems to be better.
Results of the pilot study indicate an earlier return to full mobility and shorter operating time in the IM group. This study included all intertrochanteric fracture types and did not demonstrate a clear benefit of the IM in many other parameters. The currently proposed multi-centre study will focus on the unstable A2 intertrochanteric fracture pattern.
Considering the significantly increased cost of the new intramedullary devices compared to the standard plate-hip-screw, a significant overall improvement in patient function should be realized before the general use of these new devices could be recommended.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hip Fractures
Keywords
intertrochanteric fractures
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Actual)
8. Arms, Groups, and Interventions
Arm Title
EM device
Arm Type
Active Comparator
Arm Description
Extramedullary Device (EM)
Arm Title
IM device
Arm Type
Active Comparator
Arm Description
Intramedullary Device (IM)
Intervention Type
Device
Intervention Name(s)
Dynamic Hip Screw (DHS); Trochanteric Fixation Nail (TFN)
Other Intervention Name(s)
Extramedullary plate/ screw device , Intramedullary nail
Intervention Description
Surgical stabilization of unstable intertrochanteric hip fractures using two commonly used implant categories
Primary Outcome Measure Information:
Title
Timed 2 minute walking distance
Time Frame
6 weeks, 3 months, 6 months and 12 months
Title
TUG (Time up and go) test
Time Frame
6 weeks, 3 months, 6 months and 12 months
Title
Trendelenburg's test: pelvic drop
Time Frame
6 weeks, 3 months, 6 months and 12 months
Title
Fracture classification: Mueller/ AO, displacement, time to union, heterotopic ossification and shortening.
Time Frame
6 weeks, 3 months, 6 months and 12 months
Title
FIM (Functional Independence Measure)
Time Frame
6weks, 3months, 6months and 12months
Title
LEM (Lower Extremity Measure)
Time Frame
6weeks, 3months, 6months and 12 months
Secondary Outcome Measure Information:
Title
Secondary Outcome Variable: Transfusions
Time Frame
6 weeks, 3 months, 6 months and 12 months
Title
Pre and Post operative Hgb
Time Frame
6 weeks, 3 months, 6 months and 12 months
Title
Complications/ Re-operation
Time Frame
6 weeks, 3 months, 6 months and 12 months
Title
Length of surgery and hospital stay
Time Frame
6 weeks, 3 months, 6 months and 12 months
Title
Weight bearing status post-op
Time Frame
6 weeks, 3 months, 6 months and 12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
55 years or older
Type A2 Intertrochanteric fractures
Mono trauma
Medically fit for surgery
Less than 2 weeks post fracture
Exclusion Criteria:
Fractures due to malignancy
Non-ambulatory pre-fracture
Severe dementia
Limited life expectancy due to significant medical co-morbidities
Medical contraindication to surgery
Inability to comply with rehabilitation of form completion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rudy Reindl, MD FRCSC
Organizational Affiliation
McGill University Health Centre/Research Institute of the McGill University Health Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
McGill University Health Centre - Montreal General Hospital
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3G 1A4
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
26631990
Citation
Reindl R, Harvey EJ, Berry GK, Rahme E; Canadian Orthopaedic Trauma Society (COTS). Intramedullary Versus Extramedullary Fixation for Unstable Intertrochanteric Fractures: A Prospective Randomized Controlled Trial. J Bone Joint Surg Am. 2015 Dec 2;97(23):1905-12. doi: 10.2106/JBJS.N.01007.
Results Reference
derived
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Randomized Comparison of 2 Fixation Techniques for Unstable Intertrochanteric Hip Fractures
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